Dissecting developmental disorders caused by CTCF mutation at R567 [4C]. Dissecting developmental disorders caused by CTCF mutation at R567 [4C]
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA886689
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资源简介：
In this study, we performed 4C sequencing experiments to investigate the change of chromatin interactions between the promoters of Pcdh genes and enhancers across cPcdh locus. Overall design: 4C-seq experiments were performed using wild-type and Ctcf homozygous mutated brain tissues from E18.5 mouse embryo. Two enhancers at cPcdh locus were used as viewpoints.
创建时间：
2022-10-03
